Synthesis and Insulin—sensitizing Activity of a Series of 2—Benzyl—1,3—dicarbonyl Derivatives

A series of 2-benzyl-1,3-dicabonyl derivatives was synthesized.Their insulin-sensitizing activity was evaluated in 3T3-L1 preadipocyte cells.Compounds3,26 and 27 were found to possess strong insulin-sensitizing activity in vitro and were selected for further hypoglycemic evaluation in vivo.     

聚乙撑二氧噻吩膜在氧化态的充电过程及电容研究

In this paper, the chronoamperometry was used to study the charging processes of polyethylenedioxythiophene (PEDOT) modified electrodes in the potential range where PEDOT was in the oxidized state. The results show that the charging behaviors of the PEDOT films are well agreed with the exhausted finite diffusion model. The dependence of the capacitance values of the films on potential and concentration of solution was also studied in this potential range.     

Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction

The enantioselective synthesis of the potent, selective, cytotoxic, annonaceous acetogenin, (+)-gigantecin, has been completed. An asymmetric glycolate aldol serves to establish the stereocenters at C13,14 and at C21,22. A Carreira asymmetric acetylide addition is used to establish the C17 stereocenter.     

非即变相位共轭反馈对半导体激光器动态特性的影响

从四波混频产生相位共轭的物理原因出发,定义了相位共轭镜（PCM）的响应时间．建立起非即变相位共轭反馈条件下半导体激光器的外腔模型。以响应时间及频率失调为参变量,对其分岔及噪声等动态行为进行数值分析。结果表明,不考虑噪声影响时,增加相位共轭镜响应时间会使混沌带出现的次数和范围得到较大的抑制,当响应时间增大到1．5ns时,混沌带消失,半导体激光器保持稳定的单周期状态;考虑噪声影响后,随若响应时间的相对强度噪声（RIN）可减小几dB甚至十几dB,产生突变需要的反馈量也增大一个数量级以上,且其频谱的峰值向高频方向移动;另外,由于共轭反馈引起的频率失调低于半导体激光器激射频率3个数量级以上．它只对分岔特性有影响．对相对强度噪声的影响几乎为零。     

电子照相技术成像模拟研究

针对高能电子照相的关键物理过程开展蒙特卡罗照相模拟研究,采用Geant4围绕2.5 GeV电子在四极透镜组内的输运、电子与物质相互作用衰减等照相基本过程展开研究。通过设计不同材料、不同厚度的含缺陷平板作为模拟照相客体,开展放大型电子照相系统缺陷分辨能力模拟。此外,采用不同材料、不同厚度的台阶样品,模拟获得了电子束流穿过相应面密度材料后的线扩展函数,进一步评估电子照相对实心客体的探测分辨能力。     

Stacking‐Induced Diamagnetic/Paramagnetic Conversion of Imidazo[1,2‐a]pyridin‐2(3 H)‐one Derivatives: Near‐Infrared Absorption and Magnetic Properties in the Solid State

Herein, we present three imidazo[1,2‐a]pyridin‐2(3 H)‐one derivatives that are diamagnetic in solution, but paramagnetic in the solid state, possibly owing to a stacking‐induced formation of phenoxide‐type radicals. Notably, a larger bathochromic shift of the absorption (even up to the near‐ infrared region) of these three compounds was observed in the solid state than in solution, which was attributable to the ordered columnar stacking arrangements or their single‐electron character as radicals in the solid state. Interestingly, compared to that in solution, (E)‐3‐(pyridin‐4′‐ylmethylene)imidazo[1,2‐a]pyridine 2(3 H)‐one displayed a largely red‐shifted emission (centered at 660 nm, with tailing above 800 nm) in the solid state. A larger bathochromic shift (260 nm) of the emission is an indication of better order and tight stacking in the solid state, which is brought about by the rigid and polar acceptor. These three compounds also reveal different magnetic susceptibilities at 300 K, thus implying that they possess various columnar stacking structures. Most interestingly, these three radicals exhibit unusual ferromagnetic‐to‐antiferromagnetic phase transitions, which can be attributed to anisotropic contraction and non‐uniform slippage of the columnar stacking chains.